DeltaV Automation Engineer — GMP Biotech (Switzerland)

Proclinical; Oberwallis; On-site; CHF 90,000 - 120,000; Full time

Job summary

Proclinical is seeking an Automation Engineer to design, develop, and implement Emerson DeltaV automation solutions for pharmaceutical and biotech CAPEX projects in Switzerland. The role requires GMP, GAMP, and data integrity compliance, with collaboration across cross-functional teams to deliver robust automation.

The ideal candidate has a degree in automation/electrical/computer science and hands-on DeltaV experience in pharma settings, including CSV documentation and validation activities.

Qualifications

• Degree in Automation Engineering, Electrical Engineering, Computer Science or related field.
• Experience with Emerson DeltaV automation systems in pharma/biotech environments.
• Familiarity with GMP, GAMP and CSV/documentation practices.

Responsibilities

• Design, develop and implement DeltaV automation solutions for pharma/biotech CAPEX projects.
• Configure DeltaV modules, graphics, recipes, alarms, interfaces per standards.
• Prepare and maintain validation records and GxP documentation.
• Ensure GMP, GAMP and data integrity compliance across activities.
• Support system architecture, hardware config, networking and third-party interfaces.
• Troubleshoot hardware, software and communication issues during projects and operations.
• Collaborate with process engineering, IT-OT, validation and operations teams.
• Provide technical support during startup, handover and operations.

Skills

Automation engineering

GMP compliance

GAMP knowledge

CSV (GxP)

DeltaV configuration

System integration

Troubleshooting

Project collaboration

Validation activity

Risk assessment

Education

Engineering degree (Automation/Electrical/CS)

Tools

Emerson DeltaV

Job description

Proclinical is seeking an Automation Engineer to design, develop, and implement Emerson DeltaV automation solutions for pharmaceutical and biotech CAPEX projects in Switzerland. The role requires GMP, GAMP, and data integrity compliance, with collaboration across cross-functional teams to deliver robust automation.

The ideal candidate has a degree in automation/electrical/computer science and hands-on DeltaV experience in pharma settings, including CSV documentation and validation activities.